@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_head {
  this: np:hasAssertion dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_assertion;
    np:hasProvenance dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_provenance;
    np:hasPublicationInfo dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_assertion a np:Assertion .
  
  dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_provenance a np:Provenance .
  
  dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_assertion {
  miriam-gene:59271 a ncit:C16612 .
  
  lld:C1264606 a ncit:C7057 .
  
  dgn-gda:DGNe5f040efdd6e14414a91f4b9cfb291df sio:SIO_000628 miriam-gene:59271, lld:C1264606;
    a sio:SIO_001121 .
}

dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_provenance {
  dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_assertion dcterms:description
      "[Since its discovery, human parvovirus B19 (B19V), now termed erythrovirus, has been associated with many clinical situations (neurological and myocardium infections, persistent B19V DNAemia) in addition to the prototype clinical manifestations, i.e., erythema infectiosum and erythroblastopenia crisis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:20631151;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP893375.RApxHjDiHOSQQml5njoq4uZdUMEcjSz1nCDpwRoKqbxTE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:09+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}